11p15.4 Microdeletion Associates with Hemihypertrophy.
Publication/Presentation Date
1-1-2018
Abstract
We report a preterm female infant with intrauterine growth retardation, dysmorphic facies, missing rib, small hands and feet, and hemihypertrophy. The results of whole genome SNP microarray analysis showed approximately 77 Kb interstitial deletion of the short arm of chromosome 11 (11p15.4). We report novel clinical findings of this rare genetic condition.
Volume
2018
First Page
2746347
Last Page
2746347
ISSN
2090-6544
Published In/Presented At
Puvabanditsin, S., Sadiq, M., Jacob, M., Jalil, M., Cabrera, K., Choudry, O., & Mehta, R. (2018). 11p15.4 Microdeletion Associates with Hemihypertrophy. Case reports in genetics, 2018, 2746347. https://doi.org/10.1155/2018/2746347
Disciplines
Medicine and Health Sciences | Pediatrics
PubMedID
30510815
Department(s)
Department of Pediatrics
Document Type
Article
COinS